1. To address the postulate that sublethally injured tubular cells may
be shed from renal epithelium while still viable, studies mere undert
aken in vivo in human 'acute tubular necrosis' and in rabbit models of
renal tubular injury. 2. Substantial numbers of viable tubular cells
were voided in the urine. When placed in culture, these cells gave ris
e to monolayers, confirming viability. The majority of intact cells de
monstrated markers of proximal tubule. 3. In vitro studies of human re
nal proximal tubular cells exposed to hypoxia/anoxia showed rounding a
nd retraction associated with disruption of actin microfilaments. Phal
loidin stabilized the filaments and prevented the changes in cell shap
e indicative of altered adherence.